Canonical Allele Identifier: PA2828119010
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 847453
ClinVar RCV Id: RCV001050999
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350752.1:p.Gly386Arg
CA346501317
NM_001363823.2:c.1156G>A
CA346501318
NM_001363823.2:c.1156G>C